HHSClass 3
Transcervical Contraceptive Tubal Occlusion Device
FDA adverse event reports and recall history for transcervical contraceptive tubal occlusion device (product code HHS), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 74,502
- Deaths
- 137
- Injuries
- 72,854
- Malfunctions
- 1,077
Reports per year
15312
80013
2,23614
5,95415
4,92916
11,84717
5,98318
15,08519
16,13520
3,72521
1,64022
3,63723
84824
75625
26626
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor transcervical contraceptive tubal occlusion device automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.